Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization.
about
cDNA cloning, expression and chromosomal localization of the human sarco/endoplasmic reticulum Ca(2+)-ATPase 3 geneMT-III, a brain-specific member of the metallothionein gene familyOrganization and alternate splice products of the gene encoding nuclear inhibitor of protein phosphatase-1 (NIPP-1)Detection of illegitimate rearrangement within the immunoglobulin locus on 14q32.3 in B-cell malignancies using end-sequenced probes.A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in manSaturating the region of the polycystic kidney disease gene with NotI linking clones.Isolation of a human DNA sequence which spans the fragile X.Not para-, not peri-, but centric inversion of chromosome 12.The human cadherin-10 gene: complete coding sequence, predominant expression in the brain, and mapping on chromosome 5p13-14.Diagnostic analysis of the Rubinstein-Taybi syndrome: five cosmids should be used for microdeletion detection and low number of protein truncating mutationsA mitochondrial elongation factor-like protein is over-expressed in tumours and differentially expressed in normal tissues.Detection of deletions and cryptic translocations in Miller-Dieker syndrome by in situ hybridization.Use of 3' untranslated sequences of human cDNAs for rapid chromosome assignment and conversion to STSs: implications for an expression map of the genome.Detection of Epstein-Barr virus in Hodgkin-Reed-Sternberg cells : no evidence for the persistence of integrated viral fragments inLatent membrane protein-1 (LMP-1)-negative classical Hodgkin's diseaseCytogenic and molecular analysis of an aggressive angiomyxoma.Human thrombopoietin: gene structure, cDNA sequence, expression, and chromosomal localization.A YAC contig across the fragile X site defines the region of fragility.Mspl RFLP at the D5S122 locus tightly linked to APCClosing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region.Cloning and molecular characterization of part of a new gene fused to HMGIC in mesenchymal tumors.FGFR1 gene amplification in squamous cell carcinomas of the lung: a potential favorable prognostic marker for women and for patients with advanced cancer.Rubinstein-Taybi syndrome caused by a De Novo reciprocal translocation t(2;16)(q36.3;p13.3).
P2860
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P2860
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization.
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization.
@en
type
label
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization.
@en
prefLabel
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization.
@en
P2093
P356
P1476
Rapid subchromosomal localization of cosmids by nonradioactive in situ hybridization.
@en
P2093
Breuning MH
Cornelisse CJ
Dauwerse JG
Pearson PL
van Ommen GJ
P304
P356
10.1159/000132913
P577
1990-01-01T00:00:00Z